FDA 510(k) Application Details - K192661

Device Classification Name	Polymer, Ear, Nose And Throat, Synthetic, Absorbable   More FDA Info for this Device
510(K) Number	K192661
Device Name	Polymer, Ear, Nose And Throat, Synthetic, Absorbable
Applicant	Entellus Medical, Inc. (Aka Stryker ENT) 3600 Holly Lane North, Suite 40 Plymouth, MN 55447 US Other 510(k) Applications for this Company
Contact	Karen E. Peterson Other 510(k) Applications for this Contact
Regulation Number	874.3620   More FDA Info for this Regulation Number
Classification Product Code	NHB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/25/2019
Decision Date	11/10/2019
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review